Aurelie Canal

Central Parkway
Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 21 publications

Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy.

Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy.

Journal: Neuromuscular disorders : NMD

Published: March 26, 2024

Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach.

Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach.

Journal: Frontiers in neurology

Published: December 03, 2021

Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy.

Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy.

Journal: Journal of cachexia, sarcopenia and muscle

Published: July 28, 2021

Lean regional muscle volume estimates using explanatory bioelectrical models in healthy subjects and patients with muscle wasting.

Lean regional muscle volume estimates using explanatory bioelectrical models in healthy subjects and patients with muscle wasting.

Journal: Journal of cachexia, sarcopenia and muscle

Published: May 22, 2020

Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale.

Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale.

Journal: Annals of neurology

Published: April 24, 2020

Large variation in effects during 10 years of enzyme therapy in adults with Pompe disease.

Large variation in effects during 10 years of enzyme therapy in adults with Pompe disease.

Journal: Neurology

Published: February 15, 2019

Assessment of disease progression in dysferlinopathy: A 1-year cohort study.

Assessment of disease progression in dysferlinopathy: A 1-year cohort study.

Journal: Neurology

Published: May 04, 2018

Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa.

Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa.

Journal: Molecular genetics and metabolism

Published: July 04, 2017

Cross-sectional retrospective study of muscle function in patients with glycogen storage disease type III.

Cross-sectional retrospective study of muscle function in patients with glycogen storage disease type III.

Journal: Neuromuscular disorders : NMD

Published: April 22, 2016

Multidisciplinary care allowing uneventful vaginal delivery in a woman with Pompe disease.

Multidisciplinary care allowing uneventful vaginal delivery in a woman with Pompe disease.

Journal: Neuromuscular disorders : NMD

Published: February 05, 2016

Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy.

Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy.

Journal: Neurology

Published: April 13, 2015

Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial.

Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial.

Journal: PloS one

Published: October 31, 2014

Showing 1-12 of 21

Last Updated: 09/26/2026